Incidental Mutation 'IGL00808:Tg'
ID |
14437 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Tg
|
Ensembl Gene |
ENSMUSG00000053469 |
Gene Name |
thyroglobulin |
Synonyms |
Tgn |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.116)
|
Stock # |
IGL00808
|
Quality Score |
|
Status
|
|
Chromosome |
15 |
Chromosomal Location |
66670753-66850721 bp(+) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 66683813 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Asparagine
at position 785
(Y785N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000070239
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000065916]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000065916
AA Change: Y785N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000070239 Gene: ENSMUSG00000053469 AA Change: Y785N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
TY
|
50 |
97 |
5.9e-16 |
SMART |
TY
|
118 |
165 |
5.59e-17 |
SMART |
Pfam:Thyroglobulin_1
|
174 |
252 |
4e-9 |
PFAM |
TY
|
317 |
363 |
4.36e-19 |
SMART |
low complexity region
|
495 |
504 |
N/A |
INTRINSIC |
TY
|
617 |
662 |
3.58e-15 |
SMART |
TY
|
684 |
730 |
1.47e-16 |
SMART |
TY
|
880 |
926 |
1.51e-4 |
SMART |
TY
|
1029 |
1078 |
1.21e-12 |
SMART |
TY
|
1106 |
1150 |
7.56e-5 |
SMART |
TY
|
1167 |
1215 |
7.26e-16 |
SMART |
low complexity region
|
1244 |
1255 |
N/A |
INTRINSIC |
Pfam:GCC2_GCC3
|
1464 |
1509 |
2.7e-16 |
PFAM |
TY
|
1519 |
1568 |
9.81e-13 |
SMART |
Pfam:COesterase
|
2181 |
2717 |
8.4e-140 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Thyroglobulin (Tg) is a glycoprotein homodimer produced predominantly by the thryroid gland. It acts as a substrate for the synthesis of thyroxine and triiodothyronine as well as the storage of the inactive forms of thyroid hormone and iodine. Thyroglobulin is secreted from the endoplasmic reticulum to its site of iodination, and subsequent thyroxine biosynthesis, in the follicular lumen. Mutations in this gene cause thyroid dyshormonogenesis, manifested as goiter, and are associated with moderate to severe congenital hypothyroidism. Polymorphisms in this gene are associated with susceptibility to autoimmune thyroid diseases (AITD) such as Graves disease and Hashimoto thryoiditis. [provided by RefSeq, Nov 2009] PHENOTYPE: Mice homozygous for a spontaneous mutation exhibit enlarged thyroid gland, hypothyroidism, abnormal thyroid gland morphology, and decreased body weight. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 17 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp7 |
A |
G |
7: 28,614,952 |
I297T |
probably damaging |
Het |
Agtpbp1 |
T |
C |
13: 59,462,094 |
E131G |
possibly damaging |
Het |
Ankrd12 |
A |
G |
17: 65,983,965 |
L1491S |
probably benign |
Het |
Arid4b |
T |
C |
13: 14,136,261 |
|
probably null |
Het |
Aspm |
T |
A |
1: 139,461,476 |
S626T |
probably benign |
Het |
Catsperg1 |
A |
G |
7: 29,198,146 |
S238P |
probably damaging |
Het |
Clns1a |
A |
G |
7: 97,716,514 |
H241R |
probably damaging |
Het |
Cryzl2 |
T |
C |
1: 157,470,676 |
F212L |
probably benign |
Het |
Epha5 |
A |
T |
5: 84,106,700 |
V519E |
probably damaging |
Het |
Kcnq3 |
T |
C |
15: 65,995,754 |
D680G |
possibly damaging |
Het |
Kras |
T |
C |
6: 145,246,748 |
T20A |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,335,004 |
|
probably null |
Het |
Nbas |
T |
C |
12: 13,566,120 |
|
probably benign |
Het |
Pde8a |
G |
A |
7: 81,283,014 |
|
probably null |
Het |
Rasgef1a |
A |
T |
6: 118,088,203 |
K384M |
probably damaging |
Het |
Selenov |
A |
G |
7: 28,290,426 |
S218P |
probably damaging |
Het |
Ttll13 |
G |
T |
7: 80,259,549 |
A661S |
possibly damaging |
Het |
|
Other mutations in Tg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Tg
|
APN |
15 |
66847166 |
missense |
probably damaging |
1.00 |
IGL00230:Tg
|
APN |
15 |
66827290 |
missense |
probably benign |
0.00 |
IGL00324:Tg
|
APN |
15 |
66693424 |
missense |
probably benign |
|
IGL00428:Tg
|
APN |
15 |
66773424 |
missense |
probably benign |
0.33 |
IGL00703:Tg
|
APN |
15 |
66696489 |
missense |
probably benign |
0.34 |
IGL00833:Tg
|
APN |
15 |
66688801 |
missense |
probably benign |
0.34 |
IGL00899:Tg
|
APN |
15 |
66674073 |
critical splice donor site |
probably null |
|
IGL00921:Tg
|
APN |
15 |
66764453 |
missense |
probably benign |
0.28 |
IGL00975:Tg
|
APN |
15 |
66681882 |
missense |
probably benign |
|
IGL01288:Tg
|
APN |
15 |
66736276 |
missense |
possibly damaging |
0.81 |
IGL01397:Tg
|
APN |
15 |
66696092 |
splice site |
probably benign |
|
IGL01634:Tg
|
APN |
15 |
66729566 |
missense |
probably benign |
0.34 |
IGL01646:Tg
|
APN |
15 |
66678087 |
missense |
probably damaging |
1.00 |
IGL01704:Tg
|
APN |
15 |
66671351 |
missense |
probably damaging |
0.98 |
IGL01958:Tg
|
APN |
15 |
66759486 |
missense |
probably benign |
0.06 |
IGL02093:Tg
|
APN |
15 |
66692374 |
missense |
possibly damaging |
0.83 |
IGL02113:Tg
|
APN |
15 |
66705330 |
missense |
probably benign |
0.08 |
IGL02138:Tg
|
APN |
15 |
66717233 |
missense |
probably benign |
0.01 |
IGL02156:Tg
|
APN |
15 |
66705348 |
missense |
probably benign |
0.19 |
IGL02169:Tg
|
APN |
15 |
66757943 |
missense |
probably benign |
0.04 |
IGL02342:Tg
|
APN |
15 |
66764291 |
missense |
probably benign |
|
IGL02434:Tg
|
APN |
15 |
66764342 |
missense |
probably damaging |
0.97 |
IGL02506:Tg
|
APN |
15 |
66741594 |
missense |
possibly damaging |
0.71 |
IGL02513:Tg
|
APN |
15 |
66705274 |
missense |
probably benign |
|
IGL02549:Tg
|
APN |
15 |
66839361 |
missense |
probably damaging |
1.00 |
IGL02669:Tg
|
APN |
15 |
66748726 |
splice site |
probably benign |
|
IGL02756:Tg
|
APN |
15 |
66734586 |
missense |
probably benign |
|
IGL02800:Tg
|
APN |
15 |
66757886 |
missense |
probably damaging |
1.00 |
IGL02828:Tg
|
APN |
15 |
66682394 |
missense |
probably damaging |
1.00 |
IGL02927:Tg
|
APN |
15 |
66678093 |
missense |
probably damaging |
1.00 |
IGL03061:Tg
|
APN |
15 |
66671405 |
missense |
probably damaging |
1.00 |
IGL03105:Tg
|
APN |
15 |
66715106 |
missense |
probably benign |
0.01 |
IGL03160:Tg
|
APN |
15 |
66839303 |
nonsense |
probably null |
|
IGL03242:Tg
|
APN |
15 |
66683798 |
missense |
probably damaging |
0.99 |
Also_ran
|
UTSW |
15 |
66678839 |
missense |
probably damaging |
1.00 |
bedraggled
|
UTSW |
15 |
66740714 |
missense |
probably damaging |
1.00 |
foster
|
UTSW |
15 |
66693260 |
nonsense |
probably null |
|
hognose
|
UTSW |
15 |
66717208 |
missense |
probably damaging |
0.99 |
ito
|
UTSW |
15 |
66766162 |
nonsense |
probably null |
|
ito2
|
UTSW |
15 |
66671396 |
missense |
probably damaging |
1.00 |
ito3
|
UTSW |
15 |
66773474 |
missense |
probably damaging |
1.00 |
ito4
|
UTSW |
15 |
66696520 |
missense |
possibly damaging |
0.47 |
Papua
|
UTSW |
15 |
66674050 |
missense |
probably damaging |
1.00 |
Pipistrella
|
UTSW |
15 |
66696135 |
missense |
probably damaging |
1.00 |
pluribus
|
UTSW |
15 |
66715163 |
missense |
probably damaging |
0.98 |
samarai
|
UTSW |
15 |
66758006 |
critical splice donor site |
probably null |
|
sariba
|
UTSW |
15 |
66694870 |
missense |
probably benign |
0.01 |
ticker
|
UTSW |
15 |
66827382 |
nonsense |
probably null |
|
Vampire
|
UTSW |
15 |
66682827 |
missense |
probably damaging |
1.00 |
IGL03134:Tg
|
UTSW |
15 |
66740718 |
missense |
probably damaging |
1.00 |
P0019:Tg
|
UTSW |
15 |
66688863 |
missense |
probably benign |
0.01 |
R0121:Tg
|
UTSW |
15 |
66740781 |
missense |
probably benign |
0.04 |
R0135:Tg
|
UTSW |
15 |
66694870 |
missense |
probably benign |
0.01 |
R0227:Tg
|
UTSW |
15 |
66698446 |
missense |
possibly damaging |
0.84 |
R0448:Tg
|
UTSW |
15 |
66764442 |
missense |
probably damaging |
1.00 |
R0453:Tg
|
UTSW |
15 |
66828533 |
missense |
probably benign |
0.09 |
R0504:Tg
|
UTSW |
15 |
66682404 |
missense |
probably damaging |
0.97 |
R0543:Tg
|
UTSW |
15 |
66729597 |
missense |
probably benign |
0.13 |
R0638:Tg
|
UTSW |
15 |
66717208 |
missense |
probably damaging |
0.99 |
R0639:Tg
|
UTSW |
15 |
66741484 |
critical splice acceptor site |
probably null |
|
R0646:Tg
|
UTSW |
15 |
66729626 |
missense |
probably damaging |
0.99 |
R0666:Tg
|
UTSW |
15 |
66737521 |
missense |
probably benign |
|
R0673:Tg
|
UTSW |
15 |
66741484 |
critical splice acceptor site |
probably null |
|
R0689:Tg
|
UTSW |
15 |
66839404 |
splice site |
probably benign |
|
R0704:Tg
|
UTSW |
15 |
66757880 |
missense |
probably benign |
0.02 |
R0730:Tg
|
UTSW |
15 |
66678789 |
missense |
probably damaging |
1.00 |
R0830:Tg
|
UTSW |
15 |
66725144 |
missense |
probably damaging |
1.00 |
R0959:Tg
|
UTSW |
15 |
66708010 |
missense |
probably damaging |
0.98 |
R1027:Tg
|
UTSW |
15 |
66672409 |
missense |
possibly damaging |
0.65 |
R1061:Tg
|
UTSW |
15 |
66698559 |
missense |
probably benign |
0.09 |
R1086:Tg
|
UTSW |
15 |
66684062 |
missense |
probably benign |
|
R1103:Tg
|
UTSW |
15 |
66719655 |
missense |
probably benign |
0.45 |
R1240:Tg
|
UTSW |
15 |
66828548 |
missense |
probably benign |
0.16 |
R1281:Tg
|
UTSW |
15 |
66696489 |
missense |
probably benign |
0.34 |
R1470:Tg
|
UTSW |
15 |
66849463 |
missense |
possibly damaging |
0.95 |
R1470:Tg
|
UTSW |
15 |
66849463 |
missense |
possibly damaging |
0.95 |
R1531:Tg
|
UTSW |
15 |
66850502 |
missense |
probably benign |
0.02 |
R1544:Tg
|
UTSW |
15 |
66705232 |
missense |
probably benign |
0.04 |
R1550:Tg
|
UTSW |
15 |
66693430 |
missense |
possibly damaging |
0.52 |
R1575:Tg
|
UTSW |
15 |
66729685 |
critical splice donor site |
probably null |
|
R1638:Tg
|
UTSW |
15 |
66696166 |
nonsense |
probably null |
|
R1655:Tg
|
UTSW |
15 |
66828568 |
critical splice donor site |
probably null |
|
R1671:Tg
|
UTSW |
15 |
66692387 |
missense |
possibly damaging |
0.89 |
R1789:Tg
|
UTSW |
15 |
66737548 |
missense |
probably benign |
0.00 |
R1883:Tg
|
UTSW |
15 |
66671309 |
missense |
probably damaging |
1.00 |
R1984:Tg
|
UTSW |
15 |
66682842 |
missense |
probably benign |
|
R2063:Tg
|
UTSW |
15 |
66828553 |
missense |
probably damaging |
1.00 |
R2092:Tg
|
UTSW |
15 |
66849607 |
missense |
probably null |
0.26 |
R2109:Tg
|
UTSW |
15 |
66729594 |
missense |
probably benign |
0.02 |
R2128:Tg
|
UTSW |
15 |
66694894 |
missense |
probably benign |
0.10 |
R2129:Tg
|
UTSW |
15 |
66694894 |
missense |
probably benign |
0.10 |
R2207:Tg
|
UTSW |
15 |
66681939 |
missense |
probably benign |
0.15 |
R2219:Tg
|
UTSW |
15 |
66681933 |
missense |
probably benign |
0.03 |
R2228:Tg
|
UTSW |
15 |
66674011 |
missense |
probably damaging |
0.99 |
R2229:Tg
|
UTSW |
15 |
66674011 |
missense |
probably damaging |
0.99 |
R2259:Tg
|
UTSW |
15 |
66683898 |
missense |
probably benign |
|
R2994:Tg
|
UTSW |
15 |
66681953 |
missense |
probably benign |
|
R3904:Tg
|
UTSW |
15 |
66766162 |
nonsense |
probably null |
|
R3946:Tg
|
UTSW |
15 |
66674023 |
missense |
probably damaging |
1.00 |
R3965:Tg
|
UTSW |
15 |
66684190 |
missense |
probably benign |
|
R4245:Tg
|
UTSW |
15 |
66696469 |
missense |
possibly damaging |
0.68 |
R4451:Tg
|
UTSW |
15 |
66766147 |
missense |
probably benign |
0.01 |
R4487:Tg
|
UTSW |
15 |
66671396 |
missense |
probably damaging |
1.00 |
R4489:Tg
|
UTSW |
15 |
66707942 |
missense |
probably damaging |
1.00 |
R4623:Tg
|
UTSW |
15 |
66735271 |
missense |
probably benign |
0.23 |
R4659:Tg
|
UTSW |
15 |
66673920 |
missense |
possibly damaging |
0.67 |
R4728:Tg
|
UTSW |
15 |
66682827 |
missense |
probably damaging |
1.00 |
R4760:Tg
|
UTSW |
15 |
66693319 |
missense |
probably damaging |
1.00 |
R4797:Tg
|
UTSW |
15 |
66758006 |
critical splice donor site |
probably null |
|
R4944:Tg
|
UTSW |
15 |
66764337 |
missense |
probably damaging |
1.00 |
R4998:Tg
|
UTSW |
15 |
66674050 |
missense |
probably damaging |
1.00 |
R5009:Tg
|
UTSW |
15 |
66696586 |
missense |
probably benign |
0.01 |
R5025:Tg
|
UTSW |
15 |
66707930 |
missense |
probably damaging |
1.00 |
R5035:Tg
|
UTSW |
15 |
66681813 |
splice site |
probably null |
|
R5049:Tg
|
UTSW |
15 |
66827382 |
nonsense |
probably null |
|
R5073:Tg
|
UTSW |
15 |
66735252 |
missense |
probably benign |
0.05 |
R5169:Tg
|
UTSW |
15 |
66678780 |
nonsense |
probably null |
|
R5185:Tg
|
UTSW |
15 |
66773474 |
missense |
probably damaging |
1.00 |
R5227:Tg
|
UTSW |
15 |
66759567 |
missense |
possibly damaging |
0.87 |
R5300:Tg
|
UTSW |
15 |
66678855 |
missense |
probably damaging |
1.00 |
R5334:Tg
|
UTSW |
15 |
66678055 |
missense |
probably damaging |
1.00 |
R5339:Tg
|
UTSW |
15 |
66678093 |
missense |
probably damaging |
1.00 |
R5402:Tg
|
UTSW |
15 |
66739168 |
missense |
probably damaging |
0.98 |
R5441:Tg
|
UTSW |
15 |
66696520 |
missense |
possibly damaging |
0.47 |
R5509:Tg
|
UTSW |
15 |
66827293 |
missense |
probably benign |
0.45 |
R5580:Tg
|
UTSW |
15 |
66685300 |
missense |
possibly damaging |
0.66 |
R5582:Tg
|
UTSW |
15 |
66693435 |
missense |
probably damaging |
1.00 |
R5624:Tg
|
UTSW |
15 |
66838057 |
missense |
probably benign |
0.11 |
R5686:Tg
|
UTSW |
15 |
66688889 |
missense |
probably benign |
0.28 |
R6042:Tg
|
UTSW |
15 |
66683993 |
missense |
probably benign |
0.01 |
R6122:Tg
|
UTSW |
15 |
66828457 |
missense |
probably damaging |
1.00 |
R6146:Tg
|
UTSW |
15 |
66673367 |
splice site |
probably null |
|
R6159:Tg
|
UTSW |
15 |
66735247 |
missense |
possibly damaging |
0.71 |
R6223:Tg
|
UTSW |
15 |
66707922 |
missense |
probably benign |
0.15 |
R6480:Tg
|
UTSW |
15 |
66671311 |
missense |
probably damaging |
1.00 |
R6505:Tg
|
UTSW |
15 |
66759558 |
missense |
probably damaging |
0.99 |
R6531:Tg
|
UTSW |
15 |
66839362 |
missense |
probably damaging |
0.99 |
R6614:Tg
|
UTSW |
15 |
66735259 |
missense |
probably damaging |
0.99 |
R6698:Tg
|
UTSW |
15 |
66839362 |
missense |
probably damaging |
1.00 |
R6798:Tg
|
UTSW |
15 |
66678839 |
missense |
probably damaging |
1.00 |
R6837:Tg
|
UTSW |
15 |
66696135 |
missense |
probably damaging |
1.00 |
R6861:Tg
|
UTSW |
15 |
66688891 |
missense |
probably benign |
0.00 |
R6888:Tg
|
UTSW |
15 |
66696246 |
missense |
probably damaging |
0.99 |
R6933:Tg
|
UTSW |
15 |
66764309 |
missense |
possibly damaging |
0.73 |
R6983:Tg
|
UTSW |
15 |
66693358 |
missense |
probably benign |
0.01 |
R7078:Tg
|
UTSW |
15 |
66673543 |
missense |
probably damaging |
1.00 |
R7244:Tg
|
UTSW |
15 |
66740714 |
missense |
probably damaging |
1.00 |
R7320:Tg
|
UTSW |
15 |
66694784 |
missense |
possibly damaging |
0.71 |
R7334:Tg
|
UTSW |
15 |
66725272 |
missense |
probably benign |
0.01 |
R7418:Tg
|
UTSW |
15 |
66696583 |
missense |
probably damaging |
0.99 |
R7485:Tg
|
UTSW |
15 |
66696588 |
missense |
probably benign |
0.04 |
R7524:Tg
|
UTSW |
15 |
66696161 |
missense |
probably benign |
0.01 |
R7529:Tg
|
UTSW |
15 |
66694768 |
missense |
probably damaging |
0.99 |
R7540:Tg
|
UTSW |
15 |
66689927 |
missense |
probably benign |
0.16 |
R7583:Tg
|
UTSW |
15 |
66764418 |
missense |
probably damaging |
1.00 |
R7594:Tg
|
UTSW |
15 |
66729583 |
missense |
probably benign |
0.20 |
R7667:Tg
|
UTSW |
15 |
66715163 |
missense |
probably damaging |
0.98 |
R7722:Tg
|
UTSW |
15 |
66764309 |
missense |
possibly damaging |
0.73 |
R7790:Tg
|
UTSW |
15 |
66849604 |
missense |
probably damaging |
0.99 |
R7838:Tg
|
UTSW |
15 |
66693263 |
missense |
probably benign |
0.00 |
R7890:Tg
|
UTSW |
15 |
66683814 |
missense |
probably damaging |
1.00 |
R7904:Tg
|
UTSW |
15 |
66705279 |
missense |
probably benign |
0.08 |
R7919:Tg
|
UTSW |
15 |
66684074 |
missense |
possibly damaging |
0.73 |
R7921:Tg
|
UTSW |
15 |
66683793 |
missense |
probably benign |
0.08 |
R8037:Tg
|
UTSW |
15 |
66688875 |
missense |
probably benign |
0.00 |
R8038:Tg
|
UTSW |
15 |
66688875 |
missense |
probably benign |
0.00 |
R8214:Tg
|
UTSW |
15 |
66773398 |
missense |
probably damaging |
1.00 |
R8304:Tg
|
UTSW |
15 |
66693260 |
nonsense |
probably null |
|
R8688:Tg
|
UTSW |
15 |
66694953 |
critical splice donor site |
probably benign |
|
R8709:Tg
|
UTSW |
15 |
66681937 |
missense |
probably benign |
0.08 |
R8714:Tg
|
UTSW |
15 |
66684042 |
missense |
probably damaging |
0.97 |
R8901:Tg
|
UTSW |
15 |
66685335 |
missense |
probably damaging |
1.00 |
R8917:Tg
|
UTSW |
15 |
66773483 |
critical splice donor site |
probably null |
|
R9023:Tg
|
UTSW |
15 |
66683673 |
missense |
probably damaging |
1.00 |
R9232:Tg
|
UTSW |
15 |
66698461 |
missense |
probably benign |
0.01 |
R9310:Tg
|
UTSW |
15 |
66827269 |
missense |
possibly damaging |
0.69 |
R9361:Tg
|
UTSW |
15 |
66685397 |
missense |
possibly damaging |
0.50 |
R9389:Tg
|
UTSW |
15 |
66689324 |
missense |
probably benign |
0.04 |
R9501:Tg
|
UTSW |
15 |
66847074 |
missense |
possibly damaging |
0.52 |
R9510:Tg
|
UTSW |
15 |
66674064 |
missense |
probably damaging |
1.00 |
R9594:Tg
|
UTSW |
15 |
66735260 |
nonsense |
probably null |
|
R9629:Tg
|
UTSW |
15 |
66683738 |
missense |
possibly damaging |
0.95 |
R9701:Tg
|
UTSW |
15 |
66766142 |
missense |
probably benign |
0.03 |
R9743:Tg
|
UTSW |
15 |
66689990 |
missense |
probably benign |
0.18 |
R9748:Tg
|
UTSW |
15 |
66847159 |
missense |
possibly damaging |
0.91 |
T0975:Tg
|
UTSW |
15 |
66688863 |
missense |
probably benign |
0.01 |
X0005:Tg
|
UTSW |
15 |
66688863 |
missense |
probably benign |
0.01 |
X0065:Tg
|
UTSW |
15 |
66682454 |
missense |
probably damaging |
1.00 |
X0067:Tg
|
UTSW |
15 |
66748743 |
missense |
probably benign |
0.10 |
Z1177:Tg
|
UTSW |
15 |
66685310 |
missense |
possibly damaging |
0.49 |
Z1177:Tg
|
UTSW |
15 |
66849547 |
missense |
probably benign |
0.02 |
|
Posted On |
2012-12-06 |